Condition: Osteogenesis Imperfecta · Sponsor: Assistance Publique - Hôpitaux de Paris
The aim is to determine whether vestibular deficits are present in OI, then to establish whether a correlation exists between genetic type, severity of OI and audiovestibular phenotype. OI patients aged 12 to 20 years will undergo an audiometric, immittance, and vestibular assessment. When hearing loss is conductive or mixed or in cases where vestibular deficits are identified, a CT scan without injection will be performed. In case of sensorineural hearing loss or abnormal CT results, an MRI will be performed.
This description comes directly from the study's public registry record.
Natalie Loundon, MD, PhD · 1 71 39 67 82 · natalie.loundon@aphp.fr
Hélène Morel · 1 71 19 63 46 · helene.morel@aphp.fr
Always discuss trial participation with your own doctor first.
| Hôpital Necker-Enfants Malades | Paris, France | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT05419960